A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015450



Internal ID18757984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5915640..6114652hg38UCSC Ensembl
Innerchr9:5915640..6114652hg19UCSC Ensembl
Innerchr9:5905640..6104652hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38199013
hg19199013
hg18199013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3692426
Samples
Known GenesKIAA2026, MIR4665, RANBP6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015450
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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